Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29080 | A10 | 22028536 | C | T | missense_variant | MODERATE | c.220G>A|p.Gly74Ser |
S142 |
2 | BAA10g29080 | A10 | 22028661 | G | A | missense_variant | MODERATE | c.176C>T|p.Ser59Phe |
S77 S82 |
3 | BAA10g29080 | A10 | 22029208 | G | A | upstream_gene_variant | MODIFIER | c.-214C>T| |
S219 S72 |
4 | BAA10g29080 | A10 | 22030590 | C | T | upstream_gene_variant | MODIFIER | c.-1596G>A| |
S48 |
5 | BAA10g29080 | A10 | 22032155 | C | T | upstream_gene_variant | MODIFIER | c.-3161G>A| |
S208 |
6 | BAA10g29080 | A10 | 22032800 | C | T | upstream_gene_variant | MODIFIER | c.-3806G>A| |
S67 |